ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features

Preferred Label : ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features;

Origin ID

C536182;

UMLS CUI

C1864966;

Automatic exact mappings (from CISMeF team)
- Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features [OMIM Phenotype]
Has phenotype(s) (HPO)
- High nasal bridge [HPO term]
MeSH term(s) associated for indexing
- ectodermal dysplasia [MeSH Descriptor]
- facies [MeSH Descriptor]
- hearing loss, sensorineural [MeSH Descriptor]
Record concept(s)
- ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features [OMIM Phenotype]